Evidence map›Paper›PMID 38543865›Full record

ArticleVaccines2024

Changes in the Adaptive Cellular Repertoire after Infection with Different SARS-CoV-2 VOCs in a Cohort of Vaccinated Healthcare Workers.

Sara Caldrer, Silvia Accordini, Cristina Mazzi, Natalia Tiberti, Michela Deiana, Andrea Matucci, Eleonora Rizzi, Stefano Tais, Fabio Filippo, Matteo Verzè and 6 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Sara CaldrerDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0002-2379-1082
Silvia AccordiniDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0003-1857-1429
Cristina MazziCentre for Clinical Research, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0002-4561-3447
Natalia TibertiDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0002-2981-5233
Michela DeianaDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0001-7595-2346
Andrea MatucciDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0001-9368-850X
Eleonora RizziDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.
Stefano TaisDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.
Fabio FilippoNurse Direction, IRCCS Sacro Cuore Don-Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.
Matteo VerzèMedical Direction, IRCCS Sacro Cuore Don-Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.
Paolo CattaneoDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0002-2016-3224
Gian Paolo ChiecchiDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.
Concetta CastillettiDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0001-9819-236X
Massimo DelledonneDepartment of Biotechnology, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-7100-4581
Federico GobbiDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.
Chiara PiubelliDepartment of Infectious-Tropical Diseases and Microbiology, IRCCS Sacro Cuore-Don Calabria Hospital, Negrar di Valpolicella, 37024 Verona, Italy.ORCID 0000-0002-5739-3795
Ospedale Sacro Cuore Don Calabria · ITUniversity of Verona · IT

Funding

EU funding within the MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases Project no. PE00000007, INF-ACTItalian Ministry of Health Fondi Ricerca Corrente - L1P6the Italian Ministry of Health COVID-2020-12371675
6 · The paper itself

Abstract

backgroundCurrently approved vaccines are highly effective in protecting against hospitalization and severe COVID-19 infections. How pre-existing immunity responds to new variants with mutated antigens is crucial information for elucidating the functional interplay between antibodies and B and T cell responses during infection with new SARS-CoV-2 variants.

methodsIn this study, we monitored the dynamics and persistence of the immune response versus different SARS-CoV-2 variants of concern that emerged during the pandemic period (2021-2022) in a cohort of vaccinated healthcare workers, who experienced breakthrough infection in the Pre-Delta, Delta, and Omicron waves. We evaluated both the humoral and cell-mediated responses after infection. We also evaluated the anti-SARS-CoV-2 antibodies levels produced by infection in comparison with those produced after vaccination.

resultsOur results highlighted that the immune response against the Delta VOC mainly involved an adaptive humoral and switched memory B cells component, even 3 months after the last vaccine dose, conversely showing a high percentage of depleted adaptive T cells. Omicron infections triggered a consistent production of non-vaccine-associated anti-N antibodies, probably to balance the spike epitope immune escape mechanisms.

conclusionOur results suggest a direct dependence between the VOC and different humoral and B and T cell balances in the post-infection period, despite the administration of a different number of vaccine doses and the elapsed time since the last vaccination.

Indexed as

cell-mediated immunityHCWshumoral immunitySARS-CoV-2 VOCsvaccine

Identifiers

PMID38543865
PMCPMC10974488
OpenAlexW4392096203

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.